Experimental Factor Ontology
93744 terms(s) returned
| Term Type: | Record: 90001 to 90050 of 93744 Records | Page: 1801 of 1875, First Previous Next Last | Show Records Per Page |
- threonate
- threonate measurement
- threonine
- threonine measurement
- threonine--tRNA ligase 1, cytoplasmic
- threonine--tRNA ligase 1, cytoplasmic (human)
- throat
- throat disease
- thrombin
- thrombin generation potential measurement
- thrombin measurement
- thrombin-antithrombin complex measurement
- thromboangiitis obliterans
- thromboblast
- thrombocythemia 1
- thrombocythemia 2
- thrombocythemia 3
- thrombocytopenia 1
- thrombocytopenia 10
- thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies
- thrombocytopenia 12 with or without myopathy
- thrombocytopenia 13, syndromic
- thrombocytopenia 2
- thrombocytopenia 3
- thrombocytopenia 4
- thrombocytopenia 5
- thrombocytopenia 7
- thrombocytopenia 9
- thrombocytopenia with congenital dyserythropoietic anemia
- thrombocytopenia, X-linked, with or without dyserythropoietic anemia
- thrombocytopenia, anemia, and myelofibrosis
- thrombocytopenia-Robin sequence syndrome
- thrombocytopenia-absent radius syndrome
- thrombocytopenic purpura
- thrombocytosis disease
- thrombomodulin
- thrombomodulin (human)
- thrombomodulin measurement
- thrombomodulin, signal peptide removed form
- thrombomodulin, signal peptide removed form (human)
- thrombomodulin-like receptor
- thrombomodulin-related bleeding disorder
- thrombophilia
- thrombophilia due to activated protein C resistance
- thrombophilia due to protein C deficiency, autosomal dominant
- thrombophilia due to protein C deficiency, autosomal recessive
- thrombophilia due to protein S deficiency, autosomal dominant
- thrombophilia due to protein S deficiency, autosomal recessive
- thrombophilia due to thrombin defect
- thrombophilia, X-linked, due to factor 8 defect
